Li J, Tsang B K
Department of Obstetrics and Gynaecology, University of Ottawa, Ontario, Canada.
Biol Reprod. 1995 May;52(5):1050-8. doi: 10.1095/biolreprod52.5.1050.
The present study was an examination of the possible involvement of specific membrane lipid metabolites of prostaglandins (PGs), leukotrienes (LTs), lysophosphatidic acid (LPA), and lysophosphatidyl choline (LPC) in transforming growth factor alpha-(TGF alpha) induced DNA synthesis by granulosa cells during follicular development. Granulosa cells from the first (F1) and the fifth and sixth (F5-6) largest preovulatory follicles were cultured for 18 h in the presence of TGF alpha and/or an inhibitor of either phospholipase A2 (PLA2), cyclooxygenase, or lipoxygenase, LTs, LPA, LPC, and/or PGs. TGF alpha-induced, but not basal, DNA synthesis in F1 and F5-6 granulosa cells was suppressed by inhibitors of PLA2 and cyclooxygenase but not of lipoxygenase. The inhibition was concentration-dependent and could be attenuated by exogenous PGE2. Likewise, PGF and PGE production was suppressed by these inhibitors. Moreover, PGE2 and, to a lesser extent, PGF2 alpha increased basal [3H]thymidine incorporation and enhanced DNA synthesis induced by a submaximal stimulatory concentration of TGF alpha. The mitogenic effect of PGs was more evident in granulosa cells from F5-6 follicles than in those from F1 follicles. In contrast, LTs (LTB4, LTC4, LTD4), (+)5(s)-hydroxy-(6E,8Z,11Z,14Z)-eicosatetraenoic acid (5-HETE), and lysophospholipids (LPA and LPC) had no effect on granulosa cell DNA synthesis, irrespective of the stage of ovarian follicular development and the presence of TGF alpha and PGE2. These studies demonstrate that 1) arachidonic metabolites of cyclooxygenase, but not lipoxygenase pathway and arachidonate lysophospholipid by-products (LPA and LPC), are involved in the regulation of granulosa cell DNA synthesis by TGF alpha; 2) compared to PGs of the F series, PGE2 and PGE1 are more effective in either mimicking the action of TGF alpha or potentiating the mitogenic response of the cells to the growth factor; and 3) the DNA synthetic response of the hen granulosa cell to PGs is greater in granulosa cells from F5-6 than in those from F1 follicles. These findings are consistent with our concept that an increase in PG production is a necessary element in the TGF alpha-regulated cascade of biochemical events leading to chicken granulosa cell mitogenesis during hen ovarian follicular development.
本研究旨在探讨前列腺素(PGs)、白三烯(LTs)、溶血磷脂酸(LPA)和溶血磷脂酰胆碱(LPC)等特定膜脂代谢产物在卵泡发育过程中是否参与转化生长因子α(TGFα)诱导的颗粒细胞DNA合成。将来自第一大(F1)以及第五和第六大(F5 - 6)的排卵前卵泡的颗粒细胞在TGFα和/或磷脂酶A2(PLA2)、环氧化酶或脂氧合酶、LTs、LPA、LPC和/或PGs的抑制剂存在下培养18小时。PLA2和环氧化酶抑制剂可抑制F1和F5 - 6颗粒细胞中TGFα诱导的而非基础的DNA合成,脂氧合酶抑制剂则无此作用。这种抑制作用呈浓度依赖性,且可被外源性PGE2减弱。同样,这些抑制剂也抑制了PGF和PGE的产生。此外,PGE2以及在较小程度上PGF2α增加了基础[3H]胸苷掺入,并增强了亚最大刺激浓度的TGFα诱导的DNA合成。PGs的促有丝分裂作用在F5 - 6卵泡的颗粒细胞中比在F1卵泡的颗粒细胞中更明显。相反,LTs(LTB4、LTC4、LTD4)、(+)5(s) - 羟基 - (6E,8Z,11Z,14Z) - 二十碳四烯酸(5 - HETE)以及溶血磷脂(LPA和LPC)对颗粒细胞DNA合成无影响,无论卵巢卵泡发育阶段以及TGFα和PGE2是否存在。这些研究表明:1)环氧化酶的花生四烯酸代谢产物而非脂氧合酶途径和花生四烯酸溶血磷脂副产物(LPA和LPC)参与TGFα对颗粒细胞DNA合成的调节;2)与F系列PGs相比,PGE2和PGE1在模拟TGFα的作用或增强细胞对生长因子的促有丝分裂反应方面更有效;3)母鸡颗粒细胞对PGs的DNA合成反应在F5 - 6卵泡的颗粒细胞中比在F1卵泡的颗粒细胞中更大。这些发现与我们的观点一致,即在母鸡卵巢卵泡发育过程中,PG产生的增加是TGFα调节的导致鸡颗粒细胞有丝分裂的生化事件级联反应中的一个必要因素。